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Quantitative and dynamic assessment of the contribution of the ER to phagosome formation

Authors :
Sergio Trombetta
Nicolas Touret
Paul Paroutis
Hsiao-Ping H. Moore
Christopher M. Yip
Aimin Jiang
Sergio Grinstein
James E. Shaw
Ira Mellman
Mauricio R. Terebiznik
Amy Y. M. Chow
Chantal de Chastellier
Nicole N. van der Wel
Diane Houben
Marc Pypaert
Rene E. Harrison
Peter J. Peters
Other departments
Centre d'Immunologie de Marseille - Luminy (CIML)
Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)
Guglietta, Noëlle
Source :
Cell, 123(1), 157-170. Cell Press, Cell, Cell, 2005, 123, pp.157-70, Cell, Elsevier, 2005, 123, pp.157-70
Publication Year :
2005

Abstract

SummaryPhagosomes were traditionally thought to originate from an invagination and scission of the plasma membrane to form a distinct intracellular vacuole. An alternative model implicating the endoplasmic reticulum (ER) as a major component of nascent and maturing phagosomes was recently proposed (Gagnon et al., 2002). To reconcile these seemingly disparate hypotheses, we used a combination of biochemical, fluorescence imaging, and electron microscopy techniques to quantitatively and dynamically assess the contribution of the plasmalemma and of the ER to phagosome formation and maturation. We could not verify even a transient physical continuity between the ER and the plasma membrane, nor were we able to detect a significant contribution of the ER to forming or maturing phagosomes in either macrophages or dendritic cells. Instead, our data indicate that the plasma membrane is the main constituent of nascent and newly formed phagosomes, which are progressively remodeled by fusion with endosomal and eventually lysosomal compartments as phagosomes mature into acidic, degradative organelles.

Details

Language :
English
ISSN :
00928674 and 10974172
Database :
OpenAIRE
Journal :
Cell, 123(1), 157-170. Cell Press, Cell, Cell, 2005, 123, pp.157-70, Cell, Elsevier, 2005, 123, pp.157-70
Accession number :
edsair.doi.dedup.....4c16c427e5ce67a11e0cbf292f84f17c